NDC 84293-010-01 - Whipped Gel
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 84293-010
- Requested NDC
- 84293-010-01
- Package NDCs from labels
- 84293-010-01, 84293-010-02
- Manufacturer
- OCEAN OLIVE LLC
- Effective date
- 2024-09-15
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Whipped Gel - OCEAN OLIVE LLC | OCEAN OLIVE LLC | 2024-09-15 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 84293-010-01 | Whipped Gel | 50 g in 1 CONTAINER | GEL | 50 | 1 | |
| 84293-010-02 | Whipped Gel | 1 in 1 BOX | GEL | 1 | 1 |
DailyMed Dashboard NDC Coverage#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.